Transition states for protein folding have native topologies despite high structural variability

被引:78
作者
Lindorff-Larsen, K
Vendruscolo, M
Paci, E
Dobson, CM
机构
[1] Univ Cambridge, Univ Chem Lab, Cambridge CB2 1EW, England
[2] Univ Zurich, Dept Biochem, CH-8057 Zurich, Switzerland
基金
英国惠康基金;
关键词
D O I
10.1038/nsmb765
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We present a structural analysis of the folding transition states of three SH3 domains. Our results reveal that the secondary structure is not yet fully formed at this stage of folding and that the solvent is only partially excluded from the interior of the protein. Comparison of the members of the transition state ensemble with a database of native folds shows that, despite substantial local variability, the transition state structures can all be classified as having the topology characteristic of an SH3 domain. Our results suggest a mechanism for folding in which the formation of a network of interactions among a subset of hydrophobic residues ensures that the native topology is generated. Such a mechanism enables high fidelity in folding while minimizing the need to establish a large number of specific interactions in the conformational search.
引用
收藏
页码:443 / 449
页数:7
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